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来那度胺维持治疗在新诊断的多发性骨髓瘤自体干细胞移植后的应用:一项荟萃分析。

Lenalidomide Maintenance After Autologous Stem-Cell Transplantation in Newly Diagnosed Multiple Myeloma: A Meta-Analysis.

作者信息

McCarthy Philip L, Holstein Sarah A, Petrucci Maria Teresa, Richardson Paul G, Hulin Cyrille, Tosi Patrizia, Bringhen Sara, Musto Pellegrino, Anderson Kenneth C, Caillot Denis, Gay Francesca, Moreau Philippe, Marit Gerald, Jung Sin-Ho, Yu Zhinuan, Winograd Benjamin, Knight Robert D, Palumbo Antonio, Attal Michel

机构信息

Philip L. McCarthy, Roswell Park Cancer Institute, Buffalo, NY; Sarah A. Holstein, University of Nebraska Medical Center, Omaha, NE; Maria Teresa Petrucci, University La Sapienza; Antonio Palumbo, Takeda Italia, Rome; Patrizia Tosi, Rimini Hospital, Rimini; Sara Bringhen and Francesca Gay, University of Torino, Torino; Pellegrino Musto, Cancer Institute for Research and Care and The Referral Cancer Center of Basilicata, Rionero in Vulture, Italy; Paul G. Richardson and Kenneth C. Anderson, Dana-Farber Cancer Institute, Boston, MA; Cyrille Hulin and Gerald Marit, Bordeaux Centre Hospitalier Universitaire, Bordeaux; Denis Caillot, Dijon University Hospital Center, Dijon; Philippe Moreau, University Hospital Hôtel-Dieu, Nantes; Michel Attal, Institut Universitaire du Cancer de Toulouse-Oncopole, Toulouse, France; Sin-Ho Jung, Duke University, Durham, NC; and Zhinuan Yu, Benjamin Winograd, and Robert D. Knight, Celgene Corporation, Summit, NJ.

出版信息

J Clin Oncol. 2017 Oct 10;35(29):3279-3289. doi: 10.1200/JCO.2017.72.6679. Epub 2017 Jul 25.

Abstract

Purpose Lenalidomide maintenance therapy after autologous stem-cell transplantation (ASCT) demonstrated prolonged progression-free survival (PFS) versus placebo or observation in several randomized controlled trials (RCTs) of patients with newly diagnosed multiple myeloma (NDMM). All studies had PFS as the primary end point, and none were powered for overall survival (OS) as a primary end point. Thus, a meta-analysis was conducted to better understand the impact of lenalidomide maintenance in this setting. Patients and Methods The meta-analysis was conducted using primary-source patient-level data and documentation from three RCTs (Cancer and Leukemia Group B 100104, Gruppo Italiano Malattie Ematologiche dell'Adulto RV-MM-PI-209, and Intergroupe Francophone du Myélome 2005-02) that met the following prespecified inclusion criteria: an RCT in patients with NDMM receiving ASCT followed by lenalidomide maintenance versus placebo or observation with patient-level data available and achieved database lock for primary efficacy analysis. Results Overall, 1,208 patients were included in the meta-analysis (605 patients in the lenalidomide maintenance group and 603 in the placebo or observation group). The median PFS was 52.8 months for the lenalidomide group and 23.5 months for the placebo or observation group (hazard ratio, 0.48; 95% CI, 0.41 to 0.55). At a median follow-up time of 79.5 months for all surviving patients, the median OS had not been reached for the lenalidomide maintenance group, whereas it was 86.0 months for the placebo or observation group (hazard ratio, 0.75; 95% CI, 0.63 to 0.90; P = .001). The cumulative incidence rate of a second primary malignancy before disease progression was higher with lenalidomide maintenance versus placebo or observation, whereas the cumulative incidence rates of progression, death, or death as a result of myeloma were all higher with placebo or observation versus lenalidomide maintenance. Conclusion This meta-analysis demonstrates a significant OS benefit and confirms the PFS benefit with lenalidomide maintenance after ASCT in patients with NDMM when compared with placebo or observation.

摘要

目的 在多项针对新诊断的多发性骨髓瘤(NDMM)患者的随机对照试验(RCT)中,与安慰剂或观察相比,自体干细胞移植(ASCT)后使用来那度胺维持治疗可延长无进展生存期(PFS)。所有研究均将PFS作为主要终点,且均未将总生存期(OS)作为主要终点进行效能分析。因此,进行了一项荟萃分析,以更好地了解来那度胺维持治疗在此情况下的影响。

患者与方法 使用来自三项RCT(癌症与白血病B组100104、意大利成人血液学组RV-MM-PI-209和法语国家骨髓瘤研究组2005-02)的原始患者水平数据和文档进行荟萃分析,这些研究符合以下预先设定的纳入标准:一项针对接受ASCT后使用来那度胺维持治疗与安慰剂或观察的NDMM患者的RCT,有患者水平数据且已完成主要疗效分析的数据库锁定。

结果 总体而言,荟萃分析纳入了1208例患者(来那度胺维持治疗组605例,安慰剂或观察组603例)。来那度胺组的中位PFS为52.8个月,安慰剂或观察组为23.5个月(风险比,0.48;95%CI,0.41至0.55)。在所有存活患者的中位随访时间为79.5个月时,来那度胺维持治疗组的中位OS尚未达到,而安慰剂或观察组为86.0个月(风险比,0.75;95%CI,0.63至0.90;P = 0.001)。与安慰剂或观察相比,来那度胺维持治疗在疾病进展前发生第二原发性恶性肿瘤的累积发生率更高,而安慰剂或观察组在进展、死亡或因骨髓瘤死亡的累积发生率均高于来那度胺维持治疗组。

结论 这项荟萃分析表明,与安慰剂或观察相比,NDMM患者ASCT后使用来那度胺维持治疗具有显著的OS获益,并证实了PFS获益。

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